Canonical Allele Identifier: PA915964541
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 237738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val4265Ala
CA051139
NM_000384.3:c.12794T>C